BEUDAMED
    10 results · 33ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    SCREW LOCKING

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·March 14, 2012

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·March 14, 2012

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES OBERDORF·Product code HWC·March 14, 2012

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HRS·March 14, 2012

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·March 14, 2012

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code ITI·March 19, 2013

    SCULPTRA (POLY-L-LACTIC ACID)

    FDA Adverse Event
    SANOFIAVENTIS U.S. LLC·Product code LMH·March 4, 2011

    UNK CARDIO SEAL

    FDA Adverse Event
    Injury ·NMT MEDICAL, INC.·Product code MLV·March 7, 2008

    3.5MM TI LCP® PROXIMAL HUMERU PLATE-STANDARD 3H SHAFT/90MM

    FDA Adverse Event
    Injury ·SYNTHES RARON·Product code KTW·February 16, 2016

    LATERAL DISTRACTOR

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code LXH·November 21, 2019